Raising awareness of, and supporting, young people with long-term health conditions
Hi! It feels very bizarre to introduce myself like this, but I’m Jamie, I’m 19, and I have OCD. I’ve been putting off writing this because I’m embarrassed both about having OCD and about being embarrassed. Go figure! In my title I’ve mentioned embarrassment and shame separately because in relation to my OCD, these two … Continue reading Obsessive Compulsive Disorder: stigma, embarrassment, shame.
I think that a year ago, if you had asked what I had lost and gained I would have struggled to think of what I had gained, and two years ago I would wonder why you were even asking. Now though, I feel able to think about the gains and see that they truly are … Continue reading Lost and Gained: Ally
When answering ‘what have I lost or gained because of disability?’ is difficult because I don’t have one. I have not had to deal with the struggles of diagnosis, hospital stays, and always putting my health before everything else – it hasn’t been central to my day-to-day life. I’ve never had to face the same … Continue reading Lost and Gained: Ross
Having a long term chronic illness can result in feeling like you are ‘ losing’ lots of things. Being diagnosed at a young age perhaps lessens these feelings; growing up you only pick the things which you are capable of. For instance, I never really have engaged in sport, apart from climbing from time to … Continue reading Lost and Gained: Beth
Jenny, 22 Jenny: When I got diagnosed it felt like I had gained this huge weight of responsibility, like I had this massive load to carry around with me at all times. Luckily with Type One diabetes the advancement of the medication meant that it can fit in a little case, so the weight was … Continue reading Jenny: Lost and Gained
Hospital stays are a seemingly inevitable part of having a long term health condition, and can be difficult for lots of different reasons. There’s the isolation, stress, worry, missing out on things and the fact that you usually feel completely rubbish. We are writing this, Beth and Ally as both patients and visitors, and Ross … Continue reading Managing a Hospital Stay
by Niamh Adams When you are diagnosed with a chronic illness you think the fight is over, you think you will get the help and support you need. Little did I know that this was only the start of my journey in becoming my own advocate and fighting for the support I needed. I first … Continue reading Finding The Right Doctor For You
The loneliness that came with epilepsy is one of the things that has taken me most by surprise and that I have found the hardest to manage. I feel we all know the difference between emotionally and physically alone, but it feels an important difference to emphasise. Especially because I would be doing an injustice … Continue reading In the Same Boat: Ally’s Perspective
Hi! I’m Mirren, I’m 19 years old and I’m a Gaelic student at the University of Glasgow. I suffer from seizures, usually a few times a day, and while my doctors believe they’re caused by epilepsy they are still not sure. It’s been a year and a half since I was first hospitalised, and back … Continue reading In the Same Boat: Mirren’s Perspective
Loneliness is something that we tend to talk about purely in relation to elderly people, but it is something that can affect young people too. All young people experience feelings of loneliness; growing up involves lots of challenges: moving from school to university, changes in your support system, and new experiences that can be isolating. … Continue reading Loneliness; perspectives over time.
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